Canonical Allele Identifier: CA831174551

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1353917747
• gnomAD v3: 7-107683598-TAA-T
• gnomAD v4: 7-107683598-TAA-T
• MyVariant Identifiers: chr7:g.107324044_107324045del (hg19) ; chr7:g.107683599_107683600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107683600_107683601del , CM000669.2:g.107683600_107683601del	GRCh38
NC_000007.13:g.107324045_107324046del , CM000669.1:g.107324045_107324046del	GRCh37
NC_000007.12:g.107111281_107111282del	NCBI36
NG_008489.1:g.27966_27967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1001+63_1001+64del MANE Select	ENSP00000494017.1:n.1001+63_1001+64del
ENST00000265715.7:c.1001+63_1001+64del	ENSP00000265715.3:n.1001+63_1001+64del
NM_000441.1:c.1001+63_1001+64del	NP_000432.1:n.1001+63_1001+64del
XM_005250425.1:c.1001+63_1001+64del	XP_005250482.1:n.1001+63_1001+64del
XM_006716025.2:c.1001+63_1001+64del	XP_006716088.1:n.1001+63_1001+64del
XM_005250425.2:c.1001+63_1001+64del	XP_005250482.1:n.1001+63_1001+64del
XM_006716025.3:c.1001+63_1001+64del	XP_006716088.1:n.1001+63_1001+64del
XM_017012318.1:c.1001+63_1001+64del	XP_016867807.1:n.1001+63_1001+64del
NM_000441.2:c.1001+63_1001+64del MANE Select	NP_000432.1:n.1001+63_1001+64del